Synthesize and multi-spectroscopic studies of zinc-naproxen nanodrug as DNA intercalator agent.
Cytotoxicity
DNA binding
Intercalation
Ultrasound-assisted synthesis
Zinc-naproxen nanodrug
Journal
Analytical biochemistry
ISSN: 1096-0309
Titre abrégé: Anal Biochem
Pays: United States
ID NLM: 0370535
Informations de publication
Date de publication:
01 04 2022
01 04 2022
Historique:
received:
26
05
2021
revised:
07
11
2021
accepted:
08
11
2021
pubmed:
15
11
2021
medline:
11
3
2022
entrez:
14
11
2021
Statut:
ppublish
Résumé
The zinc-naproxen complex as a nano-drug (NanoD) was synthesized successfully via effective ultrasound-assisted processes. The chemicophysical properties of the NanoD were determined using FT-IR, XRD, SEM, DLS, and EDX mapping analyses. The results confirmed the formation of the 55 nm NanoD laminates. The interaction of the obtained NanoD with calf thymus deoxyribonucleic acid (CT-DNA) was studied as well. Structural and topography changes of DNA in interaction with the NanoD were investigated by atomic force microscopy (AFM). The results of electronic absorption spectroscopy, the DNA-viscosity studies, and competition fluorescence spectroscopy showed that CT-DNA binds to the NanoD through the intercalative binding mode. The data of AFM analysis indicated swollen CT-DNA upon interaction with the NanoD. The in vitro investigation of cytotoxicity of the NanoD on HT-29, Hep G2, and B16-F10 cancer cells as well as normal HFF-1 cells. The obtained results demonstrated high cytotoxicity activity of the NanoD than that of cisplatin in the HT-29 cell line, especially at lower concentrations. On the B16-F10 cell line at lower concentrations (up to 8 μg mL
Identifiants
pubmed: 34774837
pii: S0003-2697(21)00355-9
doi: 10.1016/j.ab.2021.114454
pii:
doi:
Substances chimiques
Coordination Complexes
0
Intercalating Agents
0
Naproxen
57Y76R9ATQ
DNA
9007-49-2
calf thymus DNA
91080-16-9
Zinc
J41CSQ7QDS
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
114454Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.